BGN biglycan

Information
Symbol
BGN
Type
protein-coding
Description
biglycan
Entrez Gene ID
633
Genome
hg19
Position
chrX:152,760,438-152,775,004
Genome
hg38
Position
chrX:153,494,980-153,509,546
MIM
301870 OMIM
HGNC
HGNC:1044 HGNC
Ensembl
ENSG00000182492 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 30
Benign 0 66
Likely benign 0 240
Conflicting classifications of pathogenicity 0 22
not provided 6 0
Uncertain significance 0 308
Ranking
ClinVar
0
0
178
446
6
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM DSPG1
SYNONYM MRLS
SYNONYM PG-S1
SYNONYM PGI
SYNONYM SEMDX
SYNONYM SLRR1A
MIM 301870 OMIM
HGNC HGNC:1044 HGNC
Ensembl ENSG00000182492 Ensembl
AllianceGenome HGNC:1044
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000331595.9 hg38 chrX 153,494,980 153,509,546 14,567
ENST00000331595.9 hg19 chrX 152,760,438 152,775,004 14,567
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